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K Ricker

Showing results (91-100 of 101) with videos related to

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Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
The Journal of Clinical Investigation|April 20, 1999
Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyriaR L Lindberg, R Martini, M Baumgartner, et al.
Science (New York, N.Y.)|August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotoniaM C Koch, K Steinmeyer, C Lorenz, et al.
Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.
Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.
Neurology|December 30, 2004
Sudden cardiac death in myotonic dystrophy type 2B G H Schoser, K Ricker, C Schneider-Gold, et al.
Neurology|January 28, 1999
Linkage of proximal myotonic myopathy to chromosome 3qK Ricker, T Grimm, M C Koch, et al.
Neurology|February 26, 2003
Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrumJ W Day, K Ricker, J F Jacobsen, et al.
Human Genetics|September 1, 1996
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
The Journal of Clinical Investigation|April 20, 1999
Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyriaR L Lindberg, R Martini, M Baumgartner, et al.
Science (New York, N.Y.)|August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotoniaM C Koch, K Steinmeyer, C Lorenz, et al.
Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.
Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.
Neurology|December 30, 2004
Sudden cardiac death in myotonic dystrophy type 2B G H Schoser, K Ricker, C Schneider-Gold, et al.
Neurology|January 28, 1999
Linkage of proximal myotonic myopathy to chromosome 3qK Ricker, T Grimm, M C Koch, et al.
Neurology|February 26, 2003
Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrumJ W Day, K Ricker, J F Jacobsen, et al.
Human Genetics|September 1, 1996
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.
Pageof 11